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Doxycycline EP Impurity B

Doxycycline EP Impurity B

Product Description
CAT No.
ALN-D049003
CAS No.
3963-95-9
Mol. F.
C22H22N2O8 : HCl
Mol. Wt.
442.4 : 36.5
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Chemical Name : (4S,4aR,5S,5aR,12aS)-4-(Dimethylamino)-3,5,10,12,12a-pentahydroxy-6-methylene-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydrotetracene-2-carboxamide hydrochloride
Smiles : OC1=C2C(C([C@]3([H])C(C2=O)=C(O)[C@@]4(O)[C@@]([C@H](N(C)C)C(O)=C(C(N)=O)C4=O)([H])[C@H]3O)=C)=CC=C1.Cl
Inchi : InChI=1S/C22H24N2O8/c1-7-8-5-4-6-9(25)11(8)16(26)12-10(7)17(27)14-15(24(2)3)18(28)13(21(23)31)20(30)22(14,32)19(12)29/h4-7,10,14-15,17,25,27-29,32H,1-3H3,(H2,23,31)/t7-,10-,14-,15+,17+,22+/m1/s1
Synonym : Metacycline

Rapid liquid chromatographic method for the control of doxycycline and tiamulin residues and their metabolites in vivo assays with pigs: Treatment and depletion

By Cambeiro-Perez, Noelia; Gonzalez-Gomez, Xiana; Rey-Salgueiro, Ledicia; Simal-Gandara, Jesus; Martinez-Carballo, ElenanFrom Journal of Pharmaceutical and Biomedical Analysis (2020), 190, 113428

New HPLC-MS method for rapid and simultaneous quantification of doxycycline, diethylcarbamazine and albendazole metabolites in rat plasma and organs after concomitant oral administration

By Permana, Andi Dian; Tekko, Ismaiel A.; McCarthy, Helen O.; Donnelly, Ryan F. – From Journal of Pharmaceutical and Biomedical Analysis (2019), 170, 243-253

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